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Acta Paediatrica Scandinavica|January 1, 1982

Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.

Archives Francaises De Pediatrie|February 1, 1981

[Multiple biotin-dependent carboxylase deficiencies (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.

Archives Francaises De Pediatrie|December 1, 1979

[Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period]J M Saudubray, O Amédée-Manesme, J Lavaud, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

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Acta Paediatrica Scandinavica|January 1, 1982

Archives Francaises De Pediatrie|February 1, 1981

[Multiple biotin-dependent carboxylase deficiencies (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.

Archives Francaises De Pediatrie|December 1, 1979

[Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period]J M Saudubray, O Amédée-Manesme, J Lavaud, et al.

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